Canonical Allele Identifier: PA2573089799
Gene: SHOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1334278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031399.2:p.Ser111Phe
CA5689576
NM_007373.4:c.332C>T